Canonical Allele Identifier: CA2580101899

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154351868G>A , CM000685.2:g.154351868G>A	GRCh38
NC_000023.10:g.153580236G>A , CM000685.1:g.153580236G>A	GRCh37
NC_000023.9:g.153233430G>A	NCBI36
NG_011506.1:g.27771C>T
NG_011506.2:g.27771C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6883+16C>T	ENSP00000353467.4:n.6883+16C>T
ENST00000369850.10:c.6907+16C>T MANE Select	ENSP00000358866.3:n.6907+16C>T
ENST00000369856.8:c.6826+16C>T	ENSP00000358872.4:n.6826+16C>T
ENST00000422373.6:c.3688+16C>T	ENSP00000416926.2:n.3688+16C>T
ENST00000610817.5:c.6964+16C>T	ENSP00000480593.2:n.6964+16C>T
ENST00000673639.2:c.280-3178C>T
ENST00000676696.1:c.7186+16C>T	ENSP00000503392.1:n.7186+16C>T
ENST00000678304.1:n.2086+16C>T
ENST00000344736.8:c.6787+16C>T	ENSP00000358863.3:n.6787+16C>T
ENST00000360319.8:c.6883+16C>T	ENSP00000353467.4:n.6883+16C>T
ENST00000369850.7:c.6907+16C>T	ENSP00000358866.3:n.6907+16C>T
ENST00000369856.7:c.6826+16C>T	ENSP00000358872.4:n.6826+16C>T
ENST00000420627.5:c.6863+16C>T	ENSP00000408921.1:n.6863+16C>T
ENST00000422373.5:c.6883+16C>T	ENSP00000416926.1:n.6883+16C>T
ENST00000444578.1:c.727+16C>T	ENSP00000397824.1:n.727+16C>T
ENST00000474358.5:n.556C>T
ENST00000490936.5:n.2896+16C>T
ENST00000498411.1:n.67+949C>T
ENST00000610817.4:c.5911+16C>T	ENSP00000480593.1:n.5911+16C>T
NM_001110556.1:c.6907+16C>T	NP_001104026.1:n.6907+16C>T
NM_001456.3:c.6883+16C>T	NP_001447.2:n.6883+16C>T
XM_011531127.1:c.6811+16C>T	XP_011529429.1:n.6811+16C>T
XM_011531128.1:c.6787+16C>T	XP_011529430.1:n.6787+16C>T
XM_011531129.1:c.6733+16C>T	XP_011529431.1:n.6733+16C>T
XM_011531130.1:c.6709+16C>T	XP_011529432.1:n.6709+16C>T
XM_011531131.1:c.6706+16C>T	XP_011529433.1:n.6706+16C>T
NM_001110556.2:c.6907+16C>T MANE Select	NP_001104026.1:n.6907+16C>T
NM_001456.4:c.6883+16C>T	NP_001447.2:n.6883+16C>T